Maria Balta

• Balta, Maria; Schreurs, Olaf Joseph Franciscus; Blix, Inger Johanne Schytte & Schenck, Karl (2024). The effect of resolvin D1<inf>n-3 DPA</inf> on primary oral epithelial cell migration in vitro. European Journal of Oral Sciences. ISSN 0909-8836. doi: 10.1111/eos.12981.
• Aikaterini, Liatsi; Andreas, Agouropoulos; Balta, Maria; Athanasia, Tsiligianni & Sotiria, Gizani (2023). Long-term outcome of oral health in uncooperative children with caries treated under general anesthesia. Journal of Clinical Pediatric Dentistry. ISSN 1053-4628. 47(3), s. 64–70. doi: 10.22514/jocpd.2023.024. Fulltekst i vitenarkiv
• Balta, Maria G.; Schreurs, Olaf Joseph Franciscus; Halder, Rashi; Küntziger, Thomas M.; Sætre, Frank Ove & Blix, Inger Johanne Schytte [Vis alle 9 forfattere av denne artikkelen] (2022). RvD1n-3 DPA Downregulates the Transcription of Pro-Inflammatory Genes in Oral Epithelial Cells and Reverses Nuclear Translocation of Transcription Factor p65 after TNF-α Stimulation. International Journal of Molecular Sciences. ISSN 1661-6596. 23(23), s. 1–11. doi: 10.3390/ijms232314878. Fulltekst i vitenarkiv Vis sammendrag

  Specialized pro-resolving mediators (SPMs) are multifunctional lipid mediators that participate in the resolution of inflammation. We have recently described that oral epithelial cells (OECs) express receptors of the SPM resolvin RvD1n-3 DPA and that cultured OECs respond to RvD1n-3 DPA addition by intracellular calcium release, nuclear receptor translocation and transcription of genes coding for antimicrobial peptides. The aim of the present study was to assess the functional outcome of RvD1n-3 DPA–signaling in OECs under inflammatory conditions. To this end, we performed transcriptomic analyses of TNF-a-stimulated cells that were subsequently treated with RvD1n-3 DPA and found significant downregulation of pro-inflammatory nuclear factor kappa B (NF-kB) target genes. Further bioinformatics analyses showed that RvD1n-3 DPA inhibited the expression of several genes involved in the NF-kB activation pathway. Confocal microscopy revealed that addition of RvD1n-3 DPA to OECs reversed TNF-a-induced nuclear translocation of NF-kB p65. Co-treatment of the cells with the exportin 1 inhibitor leptomycin B indicated that RvD1n-3 DPA increases nuclear export of p65. Taken together, our observations suggest that SPMs also have the potential to be used as a therapeutic aid when inflammation is established.

• Balta, Maria; Papathanasiou, Evangelos; Blix, Inger Johanne S. & Van Dyke, T E (2021). Host Modulation and Treatment of Periodontal Disease. Journal of Dental Research. ISSN 0022-0345. 100, s. 798–809. doi: 10.1177/0022034521995157.
• Schreurs, Olaf Joseph Franciscus; Balta, Maria; Karatsaidis, Andreas & Schenck, Karl (2020). Composition of hemidesmosomes in basal keratinocytes of normal buccal mucosa and oral lichen planus. European Journal of Oral Sciences. ISSN 0909-8836. 128(5), s. 369–378. doi: 10.1111/eos.12732. Fulltekst i vitenarkiv Vis sammendrag

  Oral lichen planus (OLP) is a chronic inflammatory disease displaying ultrastructural disturbances in epithelial hemidesmosomes. The expression of several key hemidesmosomal components in OLP as well as in normal buccal mucosa is, however, unknown. The aim of the study was therefore to examine intracellular and extracellular components involved in hemidesmosomal attachment, in OLP (n = 20) and in normal buccal mucosa (n = 10), by immunofluorescence. In normal buccal mucosa, laminin‐α3γ2, integrin‐α6β4, CD151, collagen α‐1(XVII) chain, and dystonin showed linear expression along the basal membrane, indicating the presence of type I hemidesmosomes. Plectin stained most epithelial cell membranes and remained unphosphorylated at S4642. In OLP, most hemidesmosomal molecules examined showed disturbed expression consisting of discontinuous increases, apicolateral location, and/or intracellular accumulation. Plectin showed S4642‐phosphorylation at the basement membrane, and deposits of laminin‐α3 and laminin‐γ2 were found within the connective tissue. The disturbed expression of hemidesmosomal proteins in OLP indicates deficient attachment of the basal cell layer, which can contribute to detachment and cell death of basal keratinocytes seen in the disease.

• Schreurs, Olaf Joseph Franciscus; Karatsaidis, Andreas; Balta, Maria; Grung, Bjarte; Hals, Else Kristine Breivik & Schenck, Karl (2020). Expression of keratins 8, 18, and 19 in epithelia of atrophic oral lichen planus. European Journal of Oral Sciences. ISSN 0909-8836. 128(1), s. 7–17. doi: 10.1111/eos.12666. Fulltekst i vitenarkiv Vis sammendrag

  Keratins form intermediate filaments of the cytoskeleton in keratinocytes and have roles in cell structure, signaling, intracellular transport, and cell death. Oral lichen planus (OLP) is an oral inflammatory disease with derangements in basal keratinocytes and disruption of the basal membrane. Here, we focused on epithelial expression of keratins 8, 18, and 19 because these proteins are known to modulate cell death. Biopsies were taken from buccal oral mucosa of persons with normal oral mucosa (n = 10) or atrophic OLP (n = 10). Cultured normal oral keratinocytes (n = 4) showed expression of mRNA and protein for keratins 8, 18, and 19. Immunohistochemistry showed consistent staining for keratins 8 and 18 in basal keratinocytes of normal oral mucosa. In OLP, staining for keratin (K)8 was mostly negative and staining for K18 was weak. Keratin 19 was expressed irregularly in most biopsies of normal oral mucosa and not at all in OLP. Several mononuclear leukocytes in the cellular infiltrate showed membrane staining for K8 and K18. Positive staining for K16 confirmed partial collapse of the basal cell layer in OLP. The basal cell niche in OLP therefore appeared to be partly populated with keratinocytes demonstrating a higher degree of differentiation (K8− K18− K19− K16+); consequently, such areas may be more susceptible to the action of cell death factors released from the cell infiltrate as a result of lacking the protective, normal keratin present in the basal epithelial cell layer of normal oral mucosa.

• GJ Moonen, Carolyn; GD Buurma, Kirsten; RJ Faruque, Mouri; Balta, Maria; Liefferink, Erol & Bizzarro, Sergio [Vis alle 8 forfattere av denne artikkelen] (2019). Periodontal therapy increases neutrophil extracellular trap degradation. Innate Immunity. ISSN 1753-4259. doi: 10.1177/1753425919889392. Fulltekst i vitenarkiv
• Balta, Maria (2019). European survey on criteria of aesthetics for periodontal evaluation: The ESCAPE study. Journal of Clinical Periodontology. ISSN 0303-6979.
• Balta, Maria (2017). Emerging Concepts in the Resolution of Periodontal Inflammation: A Role for Resolvin E1. Frontiers in Immunology. ISSN 1664-3224. doi: 10.3389/fimmu.2017.01682.

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